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Persistence of Second and Third-Line Biologics in Inflammatory Bowel Disease: A Multi-Centre Cohort Study
被引:0
|作者:
Hanrahan, Timothy P.
[1
]
Chan, Robbie
[1
]
Tassone, Daniel
[2
]
Ding, Nik S.
[2
,3
]
Basnayake, Chamara
[2
,3
]
Schulberg, Julien
[2
]
Vasudevan, Abhinav
[1
]
Kamm, Michael
[2
,3
]
De Gregorio, Michael
[2
,3
]
van Langenberg, Daniel R.
[1
,4
]
Niewiadomski, Ola
[1
,4
]
机构:
[1] Eastern Hlth, Dept Gastroenterol, Melbourne, Vic 3128, Australia
[2] St Vincents Hosp, Dept Gastroenterol, Melbourne, Vic 3065, Australia
[3] Univ Melbourne, Melbourne Med Sch, Melbourne, Vic 3010, Australia
[4] Monash Univ, Monash Sch Med, Melbourne, Vic 3800, Australia
来源:
FUTURE PHARMACOLOGY
|
2022年
/
2卷
/
04期
关键词:
Crohn's disease;
ulcerative colitis;
infliximab;
biologics;
persistence;
ANTI-TNF THERAPY;
CROHNS-DISEASE;
INFLIXIMAB INDUCTION;
AGE;
EFFICACY;
PHARMACOKINETICS;
POLYMORPHISM;
ASSOCIATION;
GENE;
D O I:
10.3390/futurepharmacol2040041
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Background: Despite proven efficacy of biologics in inflammatory bowel disease (IBD), many exhibit primary non-response or secondary loss of response and switch to subsequent biologic(s). Here, we identified early predictors of second- and/or third-line biologic persistence in IBD, in a real-world cohort of patients. Methods: A retrospective multicentre cohort study was conducted on patients receiving second- and/or third-line biologics for IBD from 2005-2021. Cox regression was applied to identify factors predictive of longer cumulative biologic persistence prior to treatment failure. Results: Of 179 patients who received >= 2 biologics, 159 (88.8%) received an anti-tumour necrosis factor (anti-TNF) first-line. There was a significantly increased likelihood of longer treatment persistence in recipients who received an anti-TNF first, versus those that received a non-anti-TNF agent first (p < 0.01). A diagnosis of CD (OR 7.1, 95% CI [2.3-21.7], p < 0.01), and endoscopic remission achieved on the first biologic (OR 10.4 [1.3-79.9], p = 0.03) were positive predictors of longer biologic persistence, whilst advancing age at IBD diagnosis (OR 0.97 [0.94-0.99], p = 0.04) and primary non-response to initial biologic (OR 0.3 [0.1-0.7], p < 0.01) were inversely associated with biologic persistence. Conclusions: These real-world data demonstrate multiple, simple to identify factors that offer the potential for early objectively assessed response to first-line biologic to predict future biologic persistence.
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页码:669 / 680
页数:12
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